510(k) K242644 ยท DQY Catheter, Percutaneous
SENDERO MAX Delivery Catheter
| Applicant | Okami Medical, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Dec 20, 2024 |
| Received | Sep 3, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242644
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.